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FDA 510(k)

MONOJECT(R) SNAP-OVER SAFETY CAP

K-Number: K882614 · 1988-08-09

ApplicantSherwood Medical Co.
Decision Date1988-08-09
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MONOJECT(R) SNAP-OVER SAFETY CAP is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1988-08-09 under 510(k) number K882614. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOJECT(R) SNAP-OVER SAFETY CAP?

MONOJECT(R) SNAP-OVER SAFETY CAP is a medical device that received FDA 510(k) clearance on 1988-08-09. The listed applicant is Sherwood Medical Co.. The 510(k) number is K882614.

When did MONOJECT(R) SNAP-OVER SAFETY CAP receive FDA 510(k) clearance?

MONOJECT(R) SNAP-OVER SAFETY CAP received FDA 510(k) clearance on 1988-08-09, under 510(k) number K882614.

Who is the listed applicant for MONOJECT(R) SNAP-OVER SAFETY CAP?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONOJECT(R) SNAP-OVER SAFETY CAP?

The FDA product code for MONOJECT(R) SNAP-OVER SAFETY CAP is JKA.

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Other records listing Sherwood Medical Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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Related Devices (Code: JKA)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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